Results 11 to 20 of about 866,572 (335)

Systemic sclerosis and pregnancy outcomes: a retrospective study from a single center

open access: yesArthritis Research & Therapy, 2022
Background Pregnancy in systemic sclerosis (SSc) patients is no more an infrequent event as it used to be, but literature data on pregnancy outcomes in women with SSc are scarce.
Giuseppe Barilaro   +9 more
doaj   +1 more source

Association between the second-stage duration of labor and perinatal outcomes in women with a prior cesarean delivery

open access: yesBMC Pregnancy and Childbirth, 2022
Background The cesarean delivery (CD) rate has been increasing globally. Trial of labor after cesarean delivery (TOLAC) has been used as a key method for the reduction of the CD rate.
Yulian Li   +16 more
doaj   +1 more source

The application of late amniocentesis: a retrospective study in a tertiary fetal medicine center in China

open access: yesBMC Pregnancy and Childbirth, 2021
Background To assess the indications and complications of late amniocentesis and the advanced genetic test results in a tertiary university fetal medical medicine unit.
Yingting Li   +10 more
doaj   +1 more source

Rabbit neurospheres as a novel in vitro tool for studying neurodevelopmental effects induced by intrauterine growth restriction

open access: yesStem Cells Translational Medicine, 2021
The aim of this study was to develop a rabbit neurosphere culture to characterize differences in basic processes of neurogenesis induced by intrauterine growth restriction (IUGR).
Marta Barenys   +11 more
doaj   +1 more source

The association of serum total bile acid with new-onset hypertension during pregnancy

open access: yesBMC Pregnancy and Childbirth, 2022
Background There has been considerable interest in the interrelationship between the liver and hypertension. The relationship between serum total bile acid (TBA) and hypertension has been reported.
Weinan Deng   +6 more
doaj   +1 more source

Perinatal Gene Transfer to the Liver [PDF]

open access: yes, 2011
The liver acts as a host to many functions hence raising the possibility that any one may be compromised by a single gene defect. Inherited or de novo mutations in these genes may result in relatively mild diseases or be so devastating that death within
Buckley, SM   +6 more
core   +1 more source

Introducing an efficient model for the prediction of placenta accreta spectrum using the MCP regression approach based on sonography indexes: how efficient is sonography in diagnosing accreta?

open access: yesBMC Pregnancy and Childbirth, 2020
Background For the first time, we aimed to introduce a model for prediction of placenta accreta spectrum (PAS), using existing sonography indices. Methods Women with a history of Cesarean sections were included.
Mahboobeh Boroomand fard   +6 more
doaj   +1 more source

Monozygotic twins discordant for homologous Robertsonian translocation trisomy 21 of 46, XX, + 21, der (21;21) (q10; q10) in a twin-to-twin transfusion syndrome, case report

open access: yesBMC Pregnancy and Childbirth, 2021
Background Monozygotic twins are nearly identical in genotype and phenotype because monozygotic twins arise from one fertilized oocyte. In all cases of discordant karyotype in monozygotic twins, trisomy 21 accounts for about one in 385,000.
Dingya Cao   +5 more
doaj   +1 more source

Reliability of Early Fetal Echocardiography for Congenital Heart Disease Detection: A Preliminary Experience and Outcome Analysis of 102 Fetuses to Demonstrate the Value of a Clinical Flow-Chart Designed for At-Risk Pregnancy Management [PDF]

open access: yes, 2016
Early fetal echocardiography (EFEC) is a fetal cardiac ultrasound analysis performed between the 12th and 16th week of pregnancy (compared with the usual 18-22 weeks).
Abed, M.m.   +8 more
core   +1 more source

Prenatal diagnosis of Noonan syndrome in a set of monozygotic twins- a case report

open access: yesBMC Pregnancy and Childbirth, 2023
Background We report a pair of dichorionic diamniotic (DCDA) twin pregnancy affected by Noonan syndrome (NS) with a novel mutation of LZTR1 determined by genetic analysis.
Wei Jian   +6 more
doaj   +1 more source

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